280 recalls tagged with “replacement available”.
Burlington Medical recalled 14,323 Frontal Aprons sold worldwide after regulators flagged attenuation degradation over time. The aprons use Xenolite 800 shielding material. Healthcare providers should stop using the devices immediately and await instructions from Burlington Medical.
Burlington Medical recalled 402 Half Aprons sold worldwide after potential attenuation degradation. Attenuation material Xenolite 800 may degrade over time, reducing shielding lifespan. Patients and healthcare providers should stop using the aprons immediately and contact Burlington Medical for recall instructions.
Burlington Medical recalled 15,438 attenuation vests distributed worldwide after potential attenuation degradation over time. The vests use Xenolite 800 attenuation material and were produced between January 16, 2025 and January 21, 2026. Healthcare providers and patients should stop using the vest immediately and follow recall instructions.
Burlington Medical recalled 94 Kilt Blockers sold worldwide through distributors and healthcare providers. The devices may attenuate over time, shortening their lifespan. Stop using immediately and contact Burlington Medical or your healthcare provider for instructions.
Waldemar Link GmbH & Co. KG recalls 74 Embrace Drill Tower devices distributed in 15 U.S. states. The recall notes mixed-up article numbers in the overview of the instruments. The surgical steps are correct. Stop using the device immediately and follow manufacturer instructions.
Waldemar Link GmbH & Co. KG recalled 75 Embrace Shoulder Drill Tower devices distributed to U.S. hospitals after discovering mixed-up article numbers in the device overview. The surgical steps are correct, but the overview labeling is inaccurate. Healthcare providers should stop using the device immediately and follow manufacturer recall instructions sent by email.
Burlington Medical recalled 1,489 BAT Coverage units worldwide on 2026-02-11 after a design-related issue was identified. The recall targets attenuation material used in the device. The defect could affect the lifespan of the shielding. Healthcare providers and patients should stop using the device and follow manufacturer instructions. The recall is active as of 2026-04-08.
Burlington Medical, LLC recalled 103 leg wrap devices distributed worldwide through multiple retailers. The recall cites attenuation degradation over time that could shorten the devices' lifespan. Healthcare providers and patients should stop using them immediately and follow the manufacturer's recall instructions.
Burlington Medical recalled 5,198 wrap aprons worldwide after attenuation degradation was identified in Xenolite 800 material. The recall covers units manufactured between 01/16/2025 and 01/21/2026. Stop using the aprons immediately and follow the manufacturer’s recall instructions.
Burlington Medical recalled 29 Demi Half Aprons distributed worldwide after finding attenuation material may degrade over time. The degradation shortens the protective lifespan. Healthcare facilities should stop using the aprons immediately and follow the manufacturer’s recall instructions.
Burlington Medical recalled 961 caps used in medical devices sold to healthcare providers worldwide. The caps may experience attenuation degradation over time, shortening device lifespan. Healthcare providers and patients should stop using the affected caps and follow recall instructions.
Burlington Medical recalled 41,962 Thyroid Shield units worldwide after identifying attenuation degradation that could shorten the device’s lifespan. The attenuation material may degrade over time, reducing shielding effectiveness. Patients and healthcare providers should stop using the device immediately and follow the recall instructions in the manufacturer notice.
Orthalign recalled 7 drill plates used with its Lantern Knee System distributed nationwide, including Utah. The parts were manufactured out of specification and can cause a bone cut up to 0.008 inch (2.8448 mm). Healthcare providers were notified by letter and instructions to stop using the devices.
Medline recalled 108,971 units of Puracol MSC8522 and Puracol Plus MSC8622EP collagen wound dressings nationwide in the United States, with distribution to Mexico and Panama. Elevated endotoxin levels were identified in affected lots. Stop using the dressings and follow recall instructions provided by Medline or your healthcare provider.
Orthalign recalled 7 pegged drill plates used with the Lantern Knee System due to out-of-spec manufacturing that can cause bone cuts up to 2.8448 mm. The devices were distributed in Utah and across the United States. Healthcare providers and patients should stop using the device immediately and await recall instructions by letter.
Aterian recalls PurSteam Elite Travel Steamers and PurSteam Mighty Lil Steamers sold after December 2020 due to a burn risk. The steamers can expel hot water from the steam nozzle during use. Affected consumers should stop using the recalled steamers and submit a recall request at recall.pursteam.com for a full refund, which requires cutting the cord and uploading a photo of the steamer with its C
Andy & Evan recalled children’s pajama sets due to a burn hazard. The recall covers sizes 2T through 6X sold online and at multiple retailers from February 2024 through June 2025 for $13 to $58. Consumers should stop using the pajamas and seek a full refund.
Lola Plus The Boys recalls five youth hooded clothing styles sold nationwide and online at Lolaandtheboys.com from November 2022 through September 2025. Drawstrings with beads on the recalled garments can snag on objects and pose a strangulation risk. Stop using the recalled clothing now and contact Lola Plus The Boys to obtain a full refund.
Little Cow Company LLC recalled 9 oz glass jar candles sold at New Seasons Market and Town & Country stores nationwide from December 2025 through January 2026 for about $25. A glass jar may crack or break during use, creating a fire, burn and laceration risk. Stop using the recalled candles and contact Little Cow Company for a full refund.
Dresbe LED Christmas Headbands are recalled in 2026 after a battery ingestion hazard was identified. The recall covers a two-pack set labeled HB-052. Stop using the headbands and contact Dresbe for a full refund.